A pharmaceutical company in Massachusetts is looking to add a new Senior Clinical Trial Specialist to join their team in Bedford, providing logistical support for clinical trials in collaboration with cross-functional teams to ensure compliance with operational procedures and regulations.

About the Opportunity:
- Schedule: Full-time
- Hours: Standard business
- Setting: Varied clinical environments
Responsibilities:
- Managing regions/sites and CRO under the direction of a Study Lead
- Overseeing vendors, contracts, and financial forecasting
- Developing and maintaining study documents
- Contributing to the Study Management Team meetings
- Reviewing the Trial Master File and updating documents
- Performing other duties, as needed
Qualifications:
- 4 years of Clinical Research experience
- Bachelor's Degree in Healthcare and/or a Scientific-related field
- Solid understanding of Study Phases
- Solid problem-solving and time management skills
- Ability to handle multiple tasks and deadlines
Desired Qualifications:
- Master's Degree
- Certification such as CCRP
- Advanced skills in Project Management
